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(R)-1-((E)-3-Benzyloxy-propenyl)-8-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

157459-19-3

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157459-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157459-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,4,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 157459-19:
(8*1)+(7*5)+(6*7)+(5*4)+(4*5)+(3*9)+(2*1)+(1*9)=163
163 % 10 = 3
So 157459-19-3 is a valid CAS Registry Number.

157459-19-3Relevant academic research and scientific papers

Synthetic studies on quinocarcin and its related compounds. 1. Synthesis of enantiomeric pairs of the ABE ring systems of quinocarcin

Saito, Shoichi,Tamura, Osamu,Kobayashi, Yuko,Matsuda, Fuyuhiko,Katoh, Tadashi,Terashima, Shiro

, p. 6193 - 6208 (2007/10/02)

Enantiomeric pairs of the ABE ring system (5 and ent-5) and its analogues (6, ent-6, 7, and ent-7) of quinocarcin (1), a prominent antitumor antibiotic, were synthesized in >95% ee with an aim to elucidate structure-activity relationships of 1. The key st

CHIRAL SYNTHESIS OF THE ABE-RING SYSTEM OF QUINOCARCIN

Saito, Shoichi,Matsuda, Fuyuhiko,Terashima, Shiro

, p. 6301 - 6304 (2007/10/02)

An enantiomeric pair of the ABE-ring systems of quinocarcin (1), a potent antitumor antibiotic, was synthesized in > 95percent ee by employing each enantiomer of 4-O-benzyl-2,3-O-isopropylidene-threose as a chiral auxiliary and featuring novel stereoselective reduction of the 3,4-dihydroisoquinoline derivative.

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